FXIIIA and TGF-beta over-expression produces normal musculo-skeletal phenotype in TG2-/- mice

Amino Acids. 2009 Apr;36(4):679-84. doi: 10.1007/s00726-008-0133-7. Epub 2008 Jul 2.

Abstract

Transglutaminase (TGs) enzymes and proteins crosslinking have for long time been implicated in the formation of hard tissue development, matrix maturation and mineralization. Among the TGs family members, in the context of connective tissue formation, TG2 and Factor XIII are expressed in cartilage by hypertrophic chondrocytes. Here, we analyse the morphological consequences of TG2 deficiency, during the development of skeletal elements. When TG2 is absent, there are not gross abnormalities in the development of the skeletal system, probably from compensatory mechanisms resulting in increased expression of FXIIIA and TGF-beta 1. In vivo other TGs may be involved in promoting chondrocytes and osteoblast differentiation and matrix mineralisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Factor XIIIa / biosynthesis*
  • Factor XIIIa / genetics
  • GTP-Binding Proteins / deficiency*
  • GTP-Binding Proteins / genetics
  • Mice
  • Mice, Knockout
  • Muscle, Skeletal / anatomy & histology*
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism*
  • Phenotype
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transforming Growth Factor beta1 / biosynthesis*
  • Transforming Growth Factor beta1 / genetics
  • Transglutaminases / deficiency*
  • Transglutaminases / genetics

Substances

  • Transforming Growth Factor beta1
  • Factor XIIIa
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • GTP-Binding Proteins